Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
217977 | Journal of Electroanalytical Chemistry | 2016 | 5 Pages |
Abstract
•The first report of the electrochemical cyclization of Schiff bases leading to benzoxazoles using DDH as a mediator.•The presence of 2,6-lutidine facilitiates the deprotonation.•The chemistry was performed in a beaker type undivided cell under constant current electrolysis conditions.
A novel electrochemical strategy for the efficient synthesis of benzoxazoles has been developed. The chemistry is performed in a beaker-type undivided cell under constant current electrolysis conditions, utilizing 2,3-dichloro-5,6-dicyano-p-hydroquinone (DDH) as a redox catalyst.
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Chemical Engineering (General)
Authors
Li-Shuo Kang, Huan-lan Xiao, Cheng-Chu Zeng, Li-Ming Hu, R. Daniel Little,